The Medical Device Regulation (MDR) changed the European legal framework for medical devices and introduced new responsibilities for the European Medicines Agency (EMA) and for national authorities in the assessment of certain categories of products. The U.S. Commercial Service is inviting healthcare companies to join our webinar to hear directly from industry experts including: Nina Brkuljan, Senior Commercial Specialist, U.S. Mission to the European Union; and Maria Duguine, PhD Chemistry, Consultant, RQMIS (EU/UK/US regulatory consulting firm). Learn about the regulation, current implementation strategy, the certification process, time commitment and resources needed to be successful.
Who Should Attend?
- Medical device producers including (stents, catheters)
- Medication producers that use certain applicators
- Certain cosmetics and food supplement producers
Gain knowledge about MDR, how it applies to your products, and more!